Evidence map›Paper›PMID 24336724›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2013

Essential thalamic contribution to slow waves of natural sleep.

François David, Joscha T Schmiedt, Hannah L Taylor, Gergely Orban, Giuseppe Di Giovanni, Victor N Uebele, John J Renger, Régis C Lambert, Nathalie Leresche, Vincenzo Crunelli

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 114 papers.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed
9.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

114 citing papers in PubMed, 235 citations in OpenAlex.

  1. Trial
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  5. Implication of the thalamus in sleep alterations observed in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Review
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  12. Thalamic involvement defines distinct slow-wave subtypes in NREM sleep.bioRxiv : the preprint server for biology · 2025
    Article
  13. A Distinct Down-to-Up Transition Assembly in the Retrosplenial Cortex during Slow-Wave Sleep.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  14. Article
  15. Article
  16. Review
  17. Review
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  20. Review

54 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 6 countries.

François DavidNeuroscience Division, School of Biosciences, Cardiff University, Cardiff CF10 3AX, United Kingdom, Unité Mixte de Recherche 7102 Centre National de la Recherche Scientifique and Université Pierre et Marie Curie, Université Paris 6, 75005 Paris, France, Ernst Strüngmann Institute for Neuroscience in Cooperation with Max Planck Society, 60528 Frankfurt, Germany, Physiology and Biochemistry Department, Malta University, 2080 Malta, and Merck & Company Inc., West Point, Pennsylvania 19486.
Joscha T Schmiedt
Hannah L Taylor
Gergely Orban
Giuseppe Di Giovanni
Victor N Uebele
John J Renger
Régis C Lambert
Nathalie Leresche
Vincenzo Crunelli
Cardiff University · GBCentre National pour la Recherche Scientifique et Technique (CNRST) · MAUnited States Military Academy · USErnst Strüngmann Institute for Neuroscience · DESorbonne Université · FRUniversity of Malta · MT

Funding

Wellcome TrustWellcome Trust 91882
6 · The paper itself

Abstract

Slow waves represent one of the prominent EEG signatures of non-rapid eye movement (non-REM) sleep and are thought to play an important role in the cellular and network plasticity that occurs during this behavioral state. These slow waves of natural sleep are currently considered to be exclusively generated by intrinsic and synaptic mechanisms within neocortical territories, although a role for the thalamus in this key physiological rhythm has been suggested but never demonstrated. Combining neuronal ensemble recordings, microdialysis, and optogenetics, here we show that the block of the thalamic output to the neocortex markedly (up to 50%) decreases the frequency of slow waves recorded during non-REM sleep in freely moving, naturally sleeping-waking rats. A smaller volume of thalamic inactivation than during sleep is required for observing similar effects on EEG slow waves recorded during anesthesia, a condition in which both bursts and single action potentials of thalamocortical neurons are almost exclusively dependent on T-type calcium channels. Thalamic inactivation more strongly reduces spindles than slow waves during both anesthesia and natural sleep. Moreover, selective excitation of thalamocortical neurons strongly entrains EEG slow waves in a narrow frequency band (0.75-1.5 Hz) only when thalamic T-type calcium channels are functionally active. These results demonstrate that the thalamus finely tunes the frequency of slow waves during non-REM sleep and anesthesia, and thus provide the first conclusive evidence that a dynamic interplay of the neocortical and thalamic oscillators of slow waves is required for the full expression of this key physiological EEG rhythm.

Indexed as

Action PotentialsAnimalsCalcium Channels, T-TypeCerebral CortexElectroencephalographyMaleNeuronsRatsRats, WistarSleepThalamusCalcium Channels, T-Type

Identifiers

PMID24336724
PMCPMC3858629
OpenAlexW2086005261

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.